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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70156Generated: October 25, 2026

4-Nitrophenyl chloroformate → 4-Nitrophenyl 2-methylbenzo[d]thiazol-5-ylcarbamate hydrochloride

https://huagongshe.com/reaction/70156

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl chloroformateHCID 82129—
Reactant2-Methylbenzothiazol-5-ylamine dihydrochlorideHCID 16218943—
SolventSodium HydroxideHCID 14798—
Product4-Nitrophenyl 2-methylbenzo[d]thiazol-5-ylcarbamate hydrochlorideHCID 66796936—

Reaction Steps

5-Amino-2-methylbenzothiazole dihydrochloride (530 mg, 2.23 mmol) was dissolved in 1 N NaOH (10 mL) and was extracted with EtOAc (3×20 mL). The combined extracts were dried over Na2SO4, filtered, and concentrated under reduced pressure. The material was dissolved in CH2Cl2 (10 mL), p-nitrophenyl chloroformate (586 mg, 2.91 mmol) was added, and the reaction mixture was stirred at rt overnight. The resulting solid was collected by filtration, was washed with CH2Cl2, and was dried under vacuum. This gave 853 mg of the title compound contaminated with some 5-amino-2-methylbenzothiazole. LC-MS: RT=8.49 min, [M+H]+=330.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822472B2
Source datasetuspto-grants-2014_09
ORD IDord-38ab128a05964abd866f2b2fa3265fba
Source noteuspto-grants-2014_09